Zimmer Anatomical Shoulder Prosthesis, Glenoid, Cemented, sterile; REF 01.04214.370.
FDA device recall Z-1194-2007 · posted 2007-08-23 · Terminated
Recall details
- Recalling firm
- Zimmer Inc.
- Reason for recall
- The package actually contains a knee patellar implant.
- Action taken
- The firm notifed the distributor via letter dated 6/25/07, and sent by email, to retrieve the product from their customers and to return the product.
- Root cause
- Other
- Status
- Terminated
- Product code
- KWS
- Quantity affected
- 10
- Distribution
- Maryland.
- Date initiated
- 2007-06-25
- Date posted
- 2007-08-23
- Date terminated
- 2007-12-05
- Location
- Warsaw, IN
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| ANATOMICA GLENOID COMPONENT (K990136) | Sulzer Orthopedics, Inc. | 1999-03-01 |